Organic dyes, process for producing the same and use thereof

ABSTRACT

The present invention provides an organic dye, a process for producing the same and the use thereof. The organic dye has the structure of formula (I) or formula (II). The regulation of the molecular energy levels and three-dimensional structures are achieved by ring-merging phenanthrocarbazole and an electron-rich thiophene unit as well as by selecting appropriate substituents. Thereby, when the organic dye of the present invention is applied to a dye-sensitized solar cell, the power conversion efficiency of the dye-sensitized solar cell is greatly improved. Meanwhile, the raw materials for the process according to the present invention have plenty of sources with low costs, so that a commercial production can be effected.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of Chinese Application No.201510028219.7 filed on Jan. 20, 2015, the content of which is herebyincorporated by reference in its entirety.

FIELD OF THE INVENTION

The present invention relates to the field of dye-sensitized solarcells, in particular, to an organic dye, a process for producing thesame and the use thereof.

BACKGROUND OF THE INVENTION

The energy demand increases dramatically with the fast economicdevelopment in China. At present, China has become the largestenergy-importing country in the world. Furthermore, environmentalproblems accompanied with consumption of the ore-based energy, such asfog and haze, are increasingly rapidly. Therefore, it is urgent toexploit the clean and sustainable energy. As a renewable and cleanenergy source, the development and utilization of solar energy is one ofthe hotspots in the field of energy study.

As an important type of solar cells, the dye-sensitized solar cell hasbeen widely concerned all over the world. In 1991, the research group ofGrazel produced a device by adsorbing RuL₂(μ-(NC)Ru(CN)L′₂)₂(L=2,2′-bipyridyl-4,4′-dicarboxylic acid, L′=2,2′-bipyridyl), atrinuclear ruthenium dye reported by Amadelli et al as a sensitizer, ona high quality TiO₂ nano crystalline film and a power conversionefficiency of 7.1% was achieved under the simulated sunlight. Therefrom,the widely research of dye-sensitized solar cell was basking in a greatboom.

Dye-sensitized solar cells have lower manufacturing cost, variety ofcolors and good appearance compared with traditional inorganicsemiconductor solar cells. Furthermore, flexible dye-sensitized solarcells are featured with their lightweight, foldable and windableabilities, and thus can be broadly used in daily life.

At present, all of the commercial available dyes are complexescontaining a noble metal ruthenium. Due to its rare resource,Ruthenium-based materials are very expensive, which greatly limits theproduction and application thereof in large scale. Meanwhile, as anotherpromising materials, the pure organic dyes is in full flourish despitethe fact only a few devices made from pure organic dye can achieve apower conversion efficiency over 10% currently. Furthermore, theinconvenient synthesis of most of the materials used in high efficientdevices also hinders the development of the pure organic dyes indye-sensitized solar cells.

SUMMARY OF THE INVENTION

In view of above, the technical problem to be solved by the presentinvention is to provide an organic dye, which can be not only producedby a simple process, but also has a high power conversion efficiency.

The present invention provides an organic dye having the structure offormula (I) or (II):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula(IV), formula (V) or formula (VD:

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl,phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆alkoxy;

x is 0 or 1;

R₁₋₅, and R₂₋₅ are independently selected from hydrogen, aryl or C₁-C₃₆alkyl.

Preferably, the aryl is aryl substituted with C₁-C₃₆ alkyl or arylsubstituted with C₁-C₃₆ alkoxy.

Preferably, the aryl is selected from formula (VII), formula (VIII) orformula (IX):

is wherein R₈ is H, C₁-C₃₆ alkyl or C₁-C₃₆ alkoxy;

R₉, R₁₀, and R₁₁ are independently selected from H or C₁-C₃₆ alkyl;

y is 0 or 1.

Preferably, said R₁₋₁, and R₂₋₁ are independently selected from C₃-C₃₀alkyl. Preferably, said R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independentlyselected from H, C₃-C₃₀ alkyl, phenyl substituted with C₃-C₃₀ alkyl orphenyl substituted with C₃-C₃₀ alkoxy.

Preferably, said organic dye has the structure of formula (X), formula(XI) or formula (XII):

The present invention also provides a process for producing an organicdye comprising:

1) reacting a compound having the structure of formula (XIII) with acompound having the structure of formula (XIV) to give a compound havingthe structure of formula (XV):

wherein R₁ is C₁-C₃₆ alkyl;

R₅ is H, aryl or C₁-C₃₆ alkyl;

R₁₂ is C₁-C₈ alkyl;

2) converting the compound having the structure of formula (XV) to acompound having the structure of formula (I) or formula (II):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;

R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula(IV), formula (V) or formula (VI):

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl,phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆alkoxy;

x is 0 or 1;

R_(1-5,) and R₂₋₅ are independently selected from H, aryl or C₁-C₃₆alkyl.

Preferably, said step 2) specifically is as follows:

2-1) converting the compound having the structure of formula (XV) to acompound having the structure of formula (XVI) or formula (XVII):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;

R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₅, and R₂₋₅ are independently selected from H, aryl or C₁-C₃₆ alkyl;

2-2) reacting the compound having the structure of formula (XVI) orformula (XVII) with a compound having the structure of formula (XVIII)to give the compound having the structure of formula (I) or formula(II);

R₄-X (XVIII),

wherein R₄ is formula (III), formula (IV), formula (V) or formula (VT):

X is H, Br or I.

Preferably, said step 2-1) specifically is as follows:

2-1-1) converting the compound having the structure of formula (XV) intoa compound having the structure of formula (XIX):

wherein R₁ is C₁-C₃₆ alkyl;

R₂, and R₃ are independently selected from H, C₁-C₃₆ alkyl, phenylsubstituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy;

R₅ is H, aryl or C₁-C₃₆ alkyl.

2-1-2) converting the compound having the structure of formula (XIX) tothe compound having the structure of formula (XVI) or formula (XVII).

The present invention also provides a dye-sensitized solar cellcomprising an organic dye layer, wherein the organic dye layer iscomposed with the compound having the structure of formula (I) orformula (II) according to the present invention.

When compared with the prior art, the present invention provides anorganic dye having the structure of formula (I) or formula (II), whereinthe regulation and control of the molecular energy levels andthree-dimensional structures are achieved by ring-mergingphenanthrocarbazole and an electron-rich thiophene unit as well as byselecting appropriate substituents, thereby when the organic dye of thepresent invention is applied to a dye-sensitized solar cell, the powerconversion efficiency of the dye-sensitized solar cell is greatlyimproved. As shown by the results of experiments, the power conversionefficiency of the solar cell made from the organic dye according to thepresent invention can be up to 11.5%.

The present invention also provides a process for producing an organicdye, wherein phenanthrocarbazole and an electron-rich thiophene unit arering-merged by means of intramolecular cyclization, so as to achieve theconjugate extension and produce two rigid donor units. Meanwhile, theraw materials for the process of the present invention have plenty ofsources with low costs, so that the industrialized production can beeffected.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic of the structure of a dye-sensitized solar cellaccording to the present invention;

FIG. 2 is a schematic of the structure of a light absorption layer in adye-sensitized solar cell according to the present invention;

FIG. 3 is the process flow chart for the manufacture of a dye-sensitizedsolar cell according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides an organic dye having the structure offormula (I) or formula (VI):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;

R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula(IV), formula (V) or formula (VI):

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl,phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆alkoxy;

x is 0 or 1;

R₁₋₅, and R₂₋₅ are independently selected from H, aryl or C₁-C₃₆ alkyl.

According to the present invention, said R₁₋₁ is preferably C₃-C₃₀alkyl, more preferably C₅-C₂₆ alkyl, most preferably C₁₀-C₂₀ alkyl; saidR₂₋₁ is preferably C₃-C₃₀ alkyl, more preferably C₅-C₂₆ alkyl, mostpreferably C₁₀-C₂₀ alkyl;

said R₁₋₂ is preferably C₃-C₃₀ alkyl, phenyl substituted with C₃-C₃₀alkyl or phenyl substituted with C₃-C₃₀ alkoxy, more preferably C₅-C₂₆alkyl, phenyl substituted with C₅-C₂₆ alkyl or phenyl substituted withC₅-C₂₆ alkoxy, most preferably C₁₀-C₂₀ alkyl, phenyl substituted withC₃-C₂₀ alkyl or phenyl substituted with C₁₀-C₂₀ alkoxy; said R₁₋₃ ispreferably C₃-C₃₀ alkyl, phenyl substituted with C₃-C₃₀ alkyl or phenylsubstituted with C₃-C₃₀ alkoxy, more preferably C₅-C₂₆ alkyl, phenylsubstituted with C₅-C₂₆ alkyl or phenyl substituted with C₅-C₂₆ alkoxy,most preferably C₁₀-C₂₀ alkyl, phenyl substituted with C₁₀-C₂₀ alkyl orphenyl substituted with C₁₀-C₂₀ alkoxy; said R₂₋₂ is preferably C₃-C₃₀alkyl, phenyl substituted with C₃-C₃₀ alkyl or phenyl substituted withC₃-C₃₀ alkoxy, to more preferably C₅-C₂₆ alkyl, phenyl substituted withC₅-C₂₆ alkyl or phenyl substituted with C₅-C₂₆ alkoxy, most preferablyC₁₀-C₂₀ alkyl, phenyl substituted with C₁₀-C₂₀ alkyl or phenylsubstituted with C₁₀-C₂₀ alkoxy; said R₂₋₃ is preferably C₃-C₃₀ alkyl,phenyl substituted with C₃-C₃₀ alkyl or phenyl substituted with C₃-C₃₀alkoxy, more preferably C₅-C₂₆ alkyl, phenyl substituted with C₅-C₂₆alkyl or phenyl substituted with C₅-C₂₆ alkoxy, most preferably C₁₀-C₂₀alkyl, phenyl substituted with C₁₀-C₂₀ alkyl or phenyl substituted withC₁₀-C₂₀ alkoxy.

R₁₋₅ is preferably C₁-C₃₆ alkyl or aryl, said alkyl is preferably C₃-C₃₀alkyl, more preferably C₅-C₂₆ alkyl, most preferably C₁₀-C₂₀ alkyl, saidaryl is preferably an unsaturated hydrocarbyl of aryl substituted withC₁-C₃₆ alkyl or an unsaturated hydrocarbyl of aryl substituted withC₁-C₃₆ alkoxy, more preferably the aryl is preferably an unsaturatedhydrocarbyl of aryl substituted with C₃-C₃₀ alkyl or an unsaturatedhydrocarbyl of aryl substituted with C₃-C₃₀ alkoxy, most preferably thearyl is preferably an unsaturated hydrocarbyl of aryl substituted withC₅-C₂₆ alkyl or an unsaturated hydrocarbyl of aryl substituted withC₅-C₂₆ alkoxy, still most preferably the aryl is preferably anunsaturated hydrocarbyl of aryl substituted with C₁₀-C₂₀ alkyl or anunsaturated hydrocarbyl of aryl substituted with C₁₀-C₂₀ alkoxy;particularly, the aryl is formula (VII), formula (VIII) or formula (IX),

wherein R₈ is H, C₁-C₃₆ alkyl or C₁-C₃₆ alkoxy, preferably C₃-C₃₀ alkylor C₃-C₃₀ alkoxy, more preferably C₅-C₂₆ alkyl or C₅-C₂₆ alkoxy, mostpreferably C₁₀-C₂₀ alkyl or C₁₀-C₂₀ alkoxy;

R₉, R₁₀, and R₁₁ are independently selected from H or C₁-C₃₆, preferablyC₃-C₃₀ alkyl, more preferably C₅-C₂₆ alkyl, most preferably C₁₀-C₂₀alkyl;

y is 0 or 1.

said R₂₋₅ is preferably C₁-C₃₆ alkyl or aryl, said alkyl is preferablyC₃-C₃₀ alkyl, more preferably C₅-C₂₆ alkyl, most preferably C₁₀-C₂₀alkyl, said aryl is preferably an to unsaturated hydrocarbyl of arylsubstituted with C₁-C₃₆ alkyl or an unsaturated hydrocarbyl of arylsubstituted with C₁-C₃₆ alkoxy, more preferably the aryl is preferablyan unsaturated hydrocarbyl of aryl substituted with C₃-C₃₀ alkyl or anunsaturated hydrocarbyl of aryl substituted with C₃-C₃₀ alkoxy, mostpreferably the aryl is preferably an unsaturated hydrocarbyl of arylsubstituted with C₅-C₂₆ alkyl or an unsaturated hydrocarbyl of arylsubstituted with C₅-C₂₆ alkoxy, still most preferably the aryl ispreferably an unsaturated hydrocarbyl of aryl substituted with C₁₀-C₂₀alkyl or an unsaturated hydrocarbyl of aryl substituted with C₁₀-C₂₀alkoxy; particularly, the aryl is formula (VII), formula (VIII) orformula (IX):

wherein R₈ is H, C₁-C₃₆ alkyl or C₁-C₃₆ alkoxy, preferably C₃-C₃₀ alkylor C₃-C₃₀ alkoxy, more preferably C₅-C₂₆ alkyl or C₅-C₂₆ alkoxy, mostpreferably C₁₀-C₂₀ alkyl or C₁₀-C₂₀ alkoxy;

R₉, R₁₀, and R₁₁ are independently selected from H or C₁-C₃₆, preferablyC₃-C₃₀ alkyl, more preferably C₅-C₂₆ alkyl, most preferably C₁₀-C₂₀alkyl;

y is 0 or 1.

said R₆ is preferably H, C₂-C₃₀ alkyl, phenyl substituted with C₂-C₃₀alkyl or phenyl substituted with C₂-C₃₀ alkoxy, more preferably H,C₃-C₂₀ alkyl, phenyl substituted with C₃-C₂₀ alkyl or phenyl substitutedwith C₃-C₂₀ alkoxy, most preferably H, C₄-C₁₀ alkyl, phenyl substitutedwith C₄-C₁₀ alkyl or phenyl substituted with C₄-C₁₀ alkoxy, still mostpreferably H, C₅-C₈ alkyl, phenyl substituted with C₅-C₈ alkyl or phenylsubstituted with C₅-C₈ alkoxy; said R₇ is preferably H, C₂-C₃₀ alkyl,phenyl substituted with C₂-C₃₀ alkyl or phenyl substituted with C₂-C₃₀alkoxy, more preferably H, C₃-C₂₀ alkyl, phenyl substituted with C₃-C₂₀alkyl or phenyl substituted with C₃-C₂₀ alkoxy, most preferably H,C₄-C₁₀ alkyl, phenyl substituted with C₄-C₁₀ alkyl or phenyl substitutedwith C₄-C₁₀ alkoxy, still most preferably H, C₅-C₈ alkyl, phenylsubstituted with C₅-C₈ alkyl or phenyl substituted with C₅-C₈ alkoxy.

Particularly, said organic dye has the structure of formula (X), formula(XI) or formula (XII):

The present invention also provides a process for producing an organicdye, comprising:

1) reacting a compound having the structure of formula (XIII) with acompound having the structure of formula (XIV) to give a compound havingthe structure of formula (XV):

wherein R₁ is C₁-C₃₆ alkyl;

R₅ is H, aryl or C₁-C₃₆ alkyl;

R₁₂ is C₁-C₈ alkyl.

2) converting the compound having the structure of formula (XV) into acompound having the structure of formula (I) or formula (II):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula(IV), formula (V) or formula (VI):

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl,phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆alkoxy;

X is 0 or 1;

R₁₋₅, and R₂₋₅ are independently selected from hydrogen, aryl or C₁-C₃₆alkyl.

According to the present invention, a compound having the structure offormula (XIII) is reacted with a compound having the structure offormula (XIV) to give a compound having the structure of formula (XV),wherein said R₁ is preferably C₃-C₃₀ alkyl, more preferably C₅-C₂₆alkyl, most preferably C₁₀-C₂₀ alkyl; said R₅ is preferably C₁-C₃₆ alkylor aryl, said alkyl is preferably C₃-C₃₀ alkyl, more preferably C₅-C₂₆alkyl, most preferably C₁₀-C₂₀ alkyl, said aryl is preferably anunsaturated hydrocarbyl of aryl substituted with C₁-C₃₆ alkyl or anunsaturated hydrocarbyl of aryl substituted with C₁-C₃₆ alkoxy, morepreferably the aryl is preferably an unsaturated hydrocarbyl of arylsubstituted with C₃-C₃₀ alkyl or an unsaturated hydrocarbyl of arylsubstituted with C₃-C₃₀ alkoxy, most preferably the aryl is preferablyan unsaturated hydrocarbyl of aryl substituted with C₅-C₂₆ alkyl or anunsaturated hydrocarbyl of aryl substituted with C₅-C₂₆ alkoxy, stillmost preferably the aryl is preferably an unsaturated hydrocarbyl ofaryl substituted with C₁₀-C₂₀ alkyl or an unsaturated hydrocarbyl ofaryl substituted with C₁₀-C₂₀ alkoxy; particularly, the aryl is formula(VII), formula (VIII) or formula (IX); R₁₂ is preferably C₂-C₆ alkyl,more preferably C₃-C₅ alkyl.

Said compound having the structure of formula (XIII) is preferablyproduced by the following process:

reacting a compound having the structure of formula (XX) with a compoundhaving the structure of formula (XXI) to give a compound having thestructure of formula (XIII);

wherein the selection range of R₁ is ibid;

R₅-X (XXI), wherein the selection range of R₅ is ibid, X is Br—, I— or aborate ester group, preferably a borate ester group.

Particularly, the reaction catalyst is preferably Pd(OAc)₂ and anorganic phosphine ligand,2-bicyclohexylphosphino-2′,6′-dimethoxybiphenyl (Sphos); and thereaction solvent is preferably a mixed solvent of 1,4-dioxane and water;and the reaction temperature is preferably 100 to 130 ° C.

In the present invention, the source of the compound having thestructure of formula (XX) is not particularly limited, and preferably,it is synthesized in accordance with the method disclosed in W. Jiang,H. Qian, Y. Li, Z. Wang, J. Org. Chem. 2008, 73, 7369.

In order to perform the reaction better, it is perferred in the presentinvention to convert the compound having the structure of formula (XIII)into a compound having the structure of formula (XXII), and then reactit with the compound having the structure of formula (XIV) to give thecompound having the structure of formula (XV),

wherein R₁₃ is Br—, I— or Sn(CH₃)₃—.

According to the present invention, the compound having the structure offormula (XV) is converted into the compound having the structure offormula (I) or formula (II).

Particularly, it is preferred in the present invention to convert thecompound having the structure of formula (XV) into a compound having thestructure of formula (XVI) or a compound having the structure of formula(XVII) firstly by Grignard's reaction and intramolecular Friedel-Craftsalkylation reaction;

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl;

R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted withC₁-C₃₆ alkoxy;

R₁₋₅, and R₂₋₅ are independently selected from H, aryl or C₁-C₃₆ alkyl.

More particularly, it is preferred in the present invention to convertthe compound having the structure of formula (XV) into a compound havingthe structure of formula (XIX), and then convert the compound having thestructure of formula (XIX) into the compound having the structure offormula (XVI) or formula (XVII). In particular, it is preferred in thepresent invention to react the compound having the structure of formulais (XV) with a Grignard's reagent to give a compound having thestructure of formula (XIX); and then cyclize the compound having thestructure of formula (XIX) in the presence of an acid catalyst to givethe compound having the structure of formula (XVI) or formula (XVII).Said acid catalyst is preferably Amberlyst 15.

wherein R₁ is C₁-C₃₆ alkyl;

R₂, and R₃ are independently selected from H, C₁-C₃₆ alkyl, phenylsubstituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy;R₅ is H, aryl or C₁-C₃₆ alkyl.

According to the present invention, it is preferred in the presentinvention to react the compound having the structure of formula (XVI) orformula (XVII) with a compound having the structure of formula (XVIII)to give the compound having the structure of formula (I) or formula(II);

R₄-X₁ (XVIII),

wherein R₄ is formula (III), formula (IV), formula (V) or formula (VI),:

X₁ is H, Br or I.

In order to perform the reaction better, it is perferred in the presentinvention to convert the compound having the structure of formula (XVI)or the compound having the structure of formula (XVII) into a compoundhaving the structure of formula (XXIII) or formula (XXIV).

is wherein R₁₄ is preferably a leaveable group or an aldehyde group,more preferably Br—, Sn(CH₃)₃— or —CHO. Then, the compound having thestructure of formula (XXIII) or formula (XXIV) is reacted with thecompound having the structure of formula (XVIII) to give the compoundhaving the structure of formula (I) or formula (II). The reactioncatalyst used is preferably Pd₂(PPh₃)₂Cl₂, Pd₂(dba)₃/P(t-Bu)₃, orCH₃COONH₄.

The present invention also provides a dye-sensitized solar cell,comprising an organic dye layer, which contains the compound having thestructure of formula formula (I) or formula (II) according to thepresent invention. Particularly, FIGS. 1 and 2 show the structures ofdye-sensitized solar cells according to the present invention, in whichFIG. 1 is a schematic of the structure of a dye-sensitized solar cellaccording to the present invention. FIG. 2 is a schematic of thestructure of a light absorption layer in a dye-sensitized solar cellaccording to the present invention. As seen from the figures, thedye-sensitized solar cell according to the present invention consists oftransparent substrate layers 1, a conductive layer 2, a light absorptionlayer 3, a hole transport layer 6 and a counter electrode 7. Inside thetwo transparent substrate layers 1, the conductive layer 2, the lightabsorption layer 3, the hole transport layer 6 and the counter electrode7 are attached successively. The light absorption layer 3 consists of asemiconductor micro/nanoparticle layer 4 and a organic dye layer 5,wherein the semiconductor micro/nanoparticle layer 4 is attached to theconductive layer 2, while the organic dye layer 5 is attached to thehole transport layer 6.

FIG. 3 shows the manufacture process of the dye-sensitized solar cellaccording to the present invention. FIG. 3 is the process flow chart forthe manufacture of the dye-sensitized solar cell according to thepresent invention.

The present invention provides an organic dye having the structure offormula (I) or formula (II), wherein the regulation and control of themolecular energy levels and three-dimensional structures are achieved byring-merging phenanthrocarbazole and an electron-rich thiophene unit aswell as by selecting appropriate substituents, thereby when the organicdye according to the present invention is applied to a dye-sensitizedsolar cell, the photoelectric conversion efficiency of thedye-sensitized solar cell is greatly improved.

The present invention also provides a process for producing an organicdye, in which phenanthrocarbazole and an electron-rich thiophene unitare ring-merged by means of intramolecular cyclization, so as to achievethe conjugate extension and produce two rigid donor units. Meanwhile,the raw materials for the process of the present invention have plentyof sources with low costs, so that the industrialized production can beeffected.

Hereinafter, the present invention will be clearly and fully describedwith reference to the technical solutions of examples. Obviously, theexamples described are only a part of the examples of the presentinvention, rather than the whole examples. All other examples, which canbe obtained by those skilled in the art without any inventive work basedon the examples in the present invention, fall into the protection scopeof the invention.

EXAMPLE 1 Preparation of the Compound Having the Structure of Formula(X)

The compound having the structure of formula (XX) was synthesized inaccordance with the reference document (W. Jiang, H. Qian, Y. Li, Z.Wang, J. Org. Chem. 2008, 73, 7369). The compound having the structureof formula (XVIII) was is synthesized in accordance with the referencedocument (Zhang, M.; Wang, Y.; Xu, M.; Ma, W.; Li, R.; Wang, P. EnergyEnviron. Sci. 2013, 6, 2944-2949). 2-bromo-3-butyl ester thiophene waspurchased from J&K Scientific. The sources of other raw materials,solvents and catalysts used in the preparation process of the dye arenot particularly limited, and they can be generally commerciallyavailable, or prepared in accordance with the methods well-known in theart.

Synthesis of p-2-hexyldecyloxy iodobenzene

In a three-necked round-bottom flask, p-iodophenol (2.00 g) wasdissolved in 20 mL N,N-dimethyl formamide, Then 2-hexyldecyl-4-methylbenzene sulfonate (3.60 g) and potassium hydroxide (2.55 g) were addedto the reaction system. The mixture was stirred overnight at 100° C.

After completion of the reaction, the mixture was extracted three timeswith chloroform before the organic phase was washed with water and driedover anhydrous sodium sulfate. After solvent removal under reducedpressure, the crude product was purified by column chromatography(petroleum ether 60-90 ° C.) on silica gel to yield p-2-hexyldecyloxyiodobenzene (4.04 g, 97% yield).

The resultant p-2-hexyldecyloxy iodobenzene was characterized by NMR,mass spectrometry and elemental analysis, and the results were asfollows:

¹H NMR (400 MHz, CDCl₃) δ: 7.55 (d, J=8.9 Hz, 2H), 6.69 (d, J=8.9 Hz,2H), 3.80 (d, J=5.7 Hz, 2H), 1.80-1.77 (m, 1H), 1.44-1.41 (m, 4H),1.35-1.30 (m, 20H), 0.91 (t, J=6.5 Hz, 6H). ¹³C NMR (100 MHz, CDCl₃) δ:159.47, 138.30, 117.17, 82.49, 71.22, 38.09, 32.12, 32.06, 31.56, 31.54,30.22, 29.80, 29.55, 27.04, 27.02, 22.90, 14.33.

The results of mass spectrometry: 445.19 ([M+H]⁺).

The results of elemental analysis: C, 59.46; H, 8.37.

Synthesis of the compound having the structure of formula (XXI-1):

In a dry Schlenk flask, p-2-hexyldecyloxy iodobenzene (3.00 g),bis(pinacolato)diboron (2.23 g) and potassium acetate (1.19 g) weredissolved in 20 mL dimethyl sulfoxide. Then the catalyst Pd(dppf)Cl₂(247 mg) was added under the protection of argon gas. The reactionsystem was stirred at 45° C. overnight.

After completion of the reaction, the mixture was extracted three timeswith chloroform before the organic phase was washed with water and driedover anhydrous sodium sulfate. After solvent removal under reducedpressure, the crude product was purified by column chromatography(acetate/petroleum ether 60-90° C., 1/50, v/v) on silica gel to yieldthe structure of formula (XXI-1) (2.82 g, 94% yield).

The structure of the resultant compound having the structure of formula(XXI-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹H NMR (400 MHz, CDCl₃) δ: 7.76 (d, J=5.6 Hz, 2H), 6.90 (d, J=5.6 Hz,2H), 3.87 (d, J=5.7 Hz, 2H), 1.81-1.78 (m, 1H), 1.50-1.39 (m, 4H), 1.34(br, 14H), 1.28 (br, 18H), 0.90 (t, J=6.5 Hz, 6H). ¹³C NMR (100 MHz,CDCl₃) δ: 162.32, 136.69, 114.18, 83.67, 71.03, 38.20, 32.06, 31.67,30.22, 29.89, 29.78, 29.52, 27.06, 25.07, 22.87, 14.27.

The results of mass spectrometry: 444.33 ([M⁺]).

The results of elemental analysis: C, 75.64; H, 11.10.

Synthesis of the compound having the structure of formula (XIII-1):

In a three-necked round-bottom flask, the compound having the structureof formula (XX-1) (2.00 g), the compound having the structure of formula(XXI-1) (2.69 g) and potassium phosphate (4.78 g) were dissolved in amixed solvent of 20 mL 1,4-dioxane and 4 mL water. Then Pd(OAc)₂ (20 mg)and 2-bicyclohexylphosphino-2′,6′-dimethoxybiphenyl (Sphos) (37 mg),were added thereto under the protection of argon gas. The reactionsystem was stirred at 120° C. for 3 hours.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with chloroform three times. The organic phase wascombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using ethyl acetate/petroleum ether ( 1/50in volume) as the eluent to give 3.01 g of the compound having thestructure of formula (XIII-1) with a yield of 83%.

The structure of the resultant compound having the structure of formula(XIII-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹H NMR (400 MHz, CDCl₃) δ: 8.69-8.66 (m, 2H), 8.15-8.12 (m, 2H), 7.91(d, J=8.7 Hz, 1H), 7.84-8.74 (m, 3H), 7.72 (s, 1H), 7.63 (d, J=8.4 Hz,2H), 7.10 (d, J=8.4 Hz, 2H), 4.57 (d, J=7.2 Hz, 2H), 3.96 (d, J=5.5 Hz,2H), 2.31-2.30 (m, 1H), 1.88-1.84 (m, 1H), 1.60-1.51 (m, 4H), 1.47-1.27(m, 30H), 1.19-1.17 (m, 14H), 0.92-0.88 (m, 6H), 0.85-0.79 (m, 6H). ¹³CNMR (100 MHz, CDCl₃) δ: 158.98, 137.48, 134.43, 132.41, 132.32, 131.48,130.74, 130.69, 128.93, 128.24, 125.17, 125.05, 124.92, 124.65, 124.53,123.51, 120.97, 120.74, 117.59, 116.73, 114.66, 114.21, 113.59, 71.25,50.17, 40.07, 38.32, 32.17, 32.06, 31.99, 31.95, 31.71, 30.32, 30.13,29.99, 29.84, 29.71, 29.61, 29.47, 27.15, 26.66, 22.95, 22.83, 14.37,14.31, 14.26.

The results of mass spectrometry: 806.61 ([M+H]⁺).

The results of elemental analysis: C, 86.41; H, 9.86; N, 1.73.

Synthesis of the compound having the structure of formula (XXII-1-1):

In a dry Schlenk flask, the compound having the structure of formula(XIII-1) (3.00 g) was dissolved in 20 mL tetrahydrofuran. The reactionsystem was cooled to 0° C. with an ice bath. Then the N-bromosuccinimide(592 mg) was added to the reaction system, and the reaction was stirredat 0° C. for 3 hours.

After completion of the reaction, 20 mL water was added to the reactionsystem. The mixed solution was extracted with chloroform three times.The organic phase was combined, and dried over anhydrous sodiumsulphate. The desiccant was removed by filtration. The filtrate wasconcentrated, and then subjected to column chromatography by using ethylacetate/petroleum ether ( 1/20 in volume) as the eluent to give 2.80 gof the compound having the structure of formula (XXII-1-1) with a yieldof 95%.

The structure of the resultant compound having the structure of formula(XXII-1-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹H NMR (400 MHz, CDCl₃) δ: 8.45 (d, J=7.7 Hz, 1H), 8.36 (d, J=7.6 Hz,1H), 8.17 (d, J=8.2 Hz, 1H), 8.13 (d, J=8.2 Hz, 1H), 7.73 (d, J=8.0 Hz,1H), 7.69-7.66 (m, 4H), 7.51 (s, 1H), 7.20 (d, J=8.6 Hz, 2H), 4.08-4.03(m, 4H), 2.06 (br, 1H), 1.97-1.94 to (m, 1H), 1.65-1.61 (m, 4H),1.52-1.42 (m, 20H), 1.34-1.23 (m, 24H), 1.04-1.00 (m, 6H), 0.92-0.88 (m,6H). ¹³C NMR (100 MHz, CDCl₃) δ: 159.00, 137.61, 134.62, 132.10, 131.42,131.18, 130.15, 129.81, 127.83, 127.47, 124.98, 124.58, 124.48, 124.26,123.89, 121.04, 120.96, 117.09, 116.66, 116.29, 115.77, 114.64, 113.81,71.19, 49.73, 39.77, 38.34, 32.20, 32.18, 32.07, 32.00, 31.79, 31.74,30.35, 29.90, 29.81, 29.72, 29.64, 29.49, 27.18, 26.51, 22.98, 22.85,14.40, 14.33, 14.28.

The results of mass spectrometry: 884.53 ([M+H]⁺).

The results of elemental analysis: C, 78.71; H, 8.87; N, 1.59.

Synthesis of the compound having the structure of (XXII-1-2):

In a three-necked round-bottom flask dried by flame, the compound havingthe structure of formula (XXII-1-1) (2.80 g) was dissolved in 15 mLanhydrous tetrahydrofuran. The mixture was cooled to −78° C., and 2.18mL n-butyl lithium (1.6 mol/L in n-hexane) was added thereto under theprotection of argon gas. The reaction was stirred at −78° C. for 1 h,and then the trimethyl tin chloride (693 mg) was added thereto. Themixture was stirred at room temperature overnight.

After completion of the reaction, 20 mL water was added to the reactionsystem. The mixed solution was extracted with chloroform three times.The organic phase was combined, and dried over anhydrous sodiumsulphate. The desiccant was removed by filtration. The filtrate wasconcentrated to give a viscous liquid, which was directly used for thenext reaction.

Synthesis of the compound having the structure of formula (XV-1):

The compound having the structure of (XXII-1-2) was dissolved in 20 mL1,4-dioxane after sufficiently drying, and the compound 2-bromo-3-butylester thiophene (826 mg) and the catalyst Pd₂(dba)₃ (173 mg), P(t-Bu)₃(10% by mass in hexane,768 mg) and caesium fluoride (1.05 g) were addedthereto under the protection of argon gas. The reaction system wasstirred at reflux overnight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with chloroform three times. The organic phase wascombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using ethyl acetate/petroleum ether ( 1/20in volume in volume) as the eluent to give 1.95 g of the compound havingthe structure of formula (XV-1) with a yield of 63%.

The structure of the resultant compound having the structure of formula(XV-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹ _(H NMR) (400 MHz, THF-d₈) δ: 8.76-8.70 (m, 2H), 8.14-8.11 (m, 1H),7.95 (d, J=6.6 Hz, 1H), 7.84-7.78 (m, 2H), 7.75-7.71 (m, 2H), 7.69-7.67(m, 1H), 7.63-7.60 (m, 2H), 7.56-7.54 (m, 1H), 7.13-7.10 (m, 2H),4.72-4.68 (m, 2H), 4.01-3.98 (m, 2H), 3.73-3.72 (m, 2H), 2.36 (br, 1H),1.87 (br, 1H), 1.58-1.57 (m, 3H), 1.44 (br, 12H), 1.35 (br, 18H), 1.19(br, 20H), 0.91-0.90 (m, 6H), 0.83-0.78 (m, 8H). ¹³C NMR (100 MHz,THF-d₈) δ: 163.57, 160.10, 149.99, 139.22, 135.23, 133.93, 132.78,132.54, 132.18, 131.73, 131.66, 130.62, 130.11, 129.23, 129.05, 125.98,125.70, 125.57, 125.42, 124.60, 122.07, 121.72, 118.83, 117.50, 116.66,115.36, 115.13, 79.59, 71.72, 64.53, 50.64, 40.97, 40.11, 39.87, 39.37,35.65, 35.33, 33.07, 32.70, 32.66, 31.23, 30.91, 30.78, 30.66, 30.52,30.40, 30.12, 29.96, 29.08, 28.05, 27.39, 24.00, 23.69, 23.33, 23.19,21.19, 19.70, 19.65, 14.91, 14.61, 13.63, 11.90.

The results of mass spectrometry: 988.66 ([M+H]⁺).

The results of elemental analysis: C, 81.42; H, 9.09; N, 1.44.

Synthesis of the compound having the structure of formula (XIX-1):

In a three-necked round-bottom flask dried by flame, the compound havingthe to structure of formula (XV-1) (1.90 g) was dissolved in 30 mLtetrahydrofuran, and 4.81 mL n-octyl magnesium bromide solution (2 mol/Lin tetrahydrofuran) was added thereto under the protection of argon gas.The reaction system was stirred at 90° C. overnight.

After completion of the reaction, the reaction system was cooled to 0°C., and 20 mL water was added thereto. The mixed solution was extractedwith chloroform three times. The organic phase was combined, and driedover anhydrous sodium sulphate. The desiccant was removed by filtration.The filtrate was concentrated, and then subjected to columnchromatography by using chloroform/petroleum ether (⅕ in volume) as theeluent to give 1.43 g of the compound having the structure of formula(XIX-1) with a yield of 65%.

The structure of the resultant compound having the structure of formula(XIX-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.74-8.70 (m, 2H), 8.12 (d, J=8.2 Hz, 1H),7.99 (d, J=8.2 Hz, 1H), 7.92 (s, 1H), 7.82 (s, 1H), 7.75-7.71 (m, 2H),7.61 (d, J=8.4 Hz, 2H), 7.47 (d, J=5.2 Hz, 1H), 7.17 (d, J=5.2 Hz, 1H),7.11 (d, J=8.4 Hz, 2H), 4.68 (d, J=7.4 Hz, 2H), 4.00 (d, J=5.3 Hz, 2H),2.36 (br, 1H), 2.07-2.03 (m, 2H), 1.90-1.88 (m, 2H), 1.58-1.55 (m, 2H),1.44 (br, 12H), 1.36-1.29 (m, 24H), 1.20 (br, 18H), 1.09-0.97 (m, 12H),0.89-0.79 (m, 20H), 0.67 (t, J=7.2 Hz, 3H). ¹³C NMR (100 MHz, THF-d₈) δ:156.95, 149.28, 142.01, 138.67, 135.06, 133.48, 133.28, 131.72, 131.61,130.08, 129.14, 126.17, 125.81, 125.78, 125.42, 125.28, 125,21, 124.29,121.76, 121.50, 121.23, 118.41, 117.48, 116.23, 114.95, 114.57, 68.94,50.72, 40.91, 32.95, 32.89, 32.82, 32.77, 31.04, 30.80, 30.75, 30.58,30.50, 30.36, 27.47, 26.93, 23.71, 23.63, 14.60, 14.58.

The results of mass spectrometry: 1142.85 ([M+H]⁺).

The results of elemental analysis: C, 83.04; H, 10.13; N, 1.24.

Synthesis of the compound having the structure of formula (XVI-1):

In a dry three-necked round-bottom flask, the compound having thestructure of formula (XIX-1) (1.43 g) was dissolved in 30 mL toluene.Then the solid acid catalyst Amberlyst 15 (600 mg) was added thereto.The mixture was stirred at reflux under the protection of argon gasovernight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with chloroform three times. The organic phase wascombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using petroleum ether (boiling temperature:60-90° C.) as the eluent to give 843 mg of the compound having thestructure of formula (XVI-1) with a yield of 63%.

The structure of the resultant compound having the structure of formula(XVI-1) was characterized by NMR, mass spectrometry and elementalanalysis. The results were as follows:

¹ H NMR (400 MHz, THF-d₈) δ: 8.74 (dd, J₁=10.1 Hz, J₂=2.6 Hz, 2H), 8.43(d, J=7.9 Hz, 1H), 8.13 (d, J=8.1 Hz, 1H), 7.93-7.89 (m, 1H), 7.87 (s,1H), 7.77-7.73 (m, 1H), 7.62 (d, J=7.9 Hz, 2H), 7.51 (d, J=4.8 Hz, 1H),7.19 (d, J=4.0, 1H), 7.12 (d, J=7.9 Hz, 2H), 5.06 (d, J=7.4 Hz, 2H),3.99 (d, J=5.0 Hz, 2H), 2.58-2.54 (m, 3H), 2.47-2.40 (m, 2H), 1.87 (br,1H), 1.57-1.55 (m, 6H), 1.45-1.28 (m, 28H), 1.15-1.05 (m, 34H),0.93-0.89 (m, 6H), 0.82-0.74 (m, 16H). ¹³C NMR (100 MHz, THF-d₈) δ:160.05, 155.24, 142.45, 140.21, 138.13, 135.27, 134.62, 133.94, 132.40,132.15, 131.99, 131.41, 129.25, 127.60, 125.85, 125.78, 125.73, 125.56,125.40, 125.13, 123.08, 121.71, 121.40, 118.92, 118.27, 116.15, 115.39,71.65, 54.10, 40.63, 40.37, 39.33, 33.06, 32.89, 32.63, 31.23, 31.04,30.90, 30.78, 30.56, 30.50, 30.40, 28.03, 27.96, 25.16, 23.77, 23.63,23.58, 14.69, 14.62, 14.56.

The results of mass spectrometry: 1124.85 ([M+H]⁺).

The results of elemental analysis: C, 84.34; H, 10.13; N, 1.24.

Synthesis of the compound having the structure of formula (XXIII-1):

In a three-necked round-bottom flask dried by flame, the compound havingthe structure of formula (XVI-1) (800 mg) was dissolved in 15 mLanhydrous tetrahydrofuran. The mixture was cooled to −78° C., andt-butyl lithium (0.66 mL, 1.3 mol/L in n-hexane) was added thereto underthe protection of argon gas. The reaction was stirred at −78° C. for 1h, and then trimethyl tin chloride (169 mg) was added thereto. Themixture was stirred at room temperature overnight.

After completion of the reaction, 20 mL water was added to the reactionsystem. The mixed solution was extracted with chloroform three times.The organic phase was combined, and dried over anhydrous sodiumsulphate. The desiccant was removed by filtration. The filtrate wasconcentrated to give a viscous liquid, which was directly used for thenext reaction.

Synthesis of the compound having the structure of formula (X-1):

The compound having the structure of formula (XXIII-1) was dissolved in20 mL 1,4-dioxane after sufficiently drying. Then the compound havingthe structure of formula (XVIII-1) (500 mg) and the catalystPd(PPh₃)₂Cl₂ (60 mg) were added thereto under the protection of argongas. The reaction system was stirred at reflux overnight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with chloroform three times. The organic phases werecombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using ethyl acetate/petroleum ether ( 1/20in volume) as the eluent to give 825 mg of the compound having thestructure of formula (X-1) with a yield of 81%.

The structure of the resultant compound having the structure of formula(X-1) was characterized by NMR, mass spectrometry and elementalanalysis. The characterization data of NMR were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.75 (m, 2H), 8.54 (m, 1H), 8.51 (s, 1H),8.18 (m, 6H), 7.98 (m, 3H), 7.77 (m, 1H), 7.62 (d, J=7.8 Hz, 2H), 7.13(d, J=8.6 Hz, 2H), 5.09 (m, 2H), 4.36 (t, J=6.5 Hz, 2H), 4.00 (d, J=5.0Hz, 2H), 2.66 (m, 2H), 2.58 (m, 3H), 1.88 (m, 1H), 1.79 (m, 2H), 1.54(m, 6H), 1.46-1.29 (m, 30H), 1.17 (m, 20H), 1.04 (m, 20H), 0.91 (m, 8H),0.80-0.74 (m, 7H), 0.69 (t, J=6.4 Hz, 6H). ¹³C NMR (100 MHz, CDCl₃) δ:166.54, 160.11, 156.18, 154.91, 153.63, 145.42, 142.55, 142.17, 140.88,138.69, 135.16, 134.44, 132.27, 132.17, 131.99, 131.26, 130.94, 130.39,129.93, 129.72, 129.25, 126.12, 125.81, 125.67, 125.59, 125.28, 124.81,123.28, 122.56, 121.95, 121.52, 119.01, 118.87, 116.16, 115.42, 71.68,65.40, 67.15, 54.18, 40.69, 40.45, 39.34, 33.06, 32.94, 32.89, 32.63,32.04, 31.24, 30.90, 30.82, 30.78, 30.60, 30.50, 30.45, 30.39, 28.03,25.40, 23.76, 23.64, 23.55, 20.37, 14.67, 14.62, 14.56, 14.50, 14.36.

The results of mass spectrometry: 1435.95 ([M+H]⁺).

The results of elemental analysis: C, 80.34; H, 8.91; N, 2.91.

Synthesis of the compound having the structure of formula (X):

In a three-necked round-bottom flask, the compound having the structureof formula (X-1) (600 mg) was dissolved in 15 mL tetrahydrofuran and 5mL water. Then the potassium hydroxide (235 mg) was added to thereaction system. The mixture was stirred at 80° C. for 5 hours.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL aqueous phosphoric acid solution (0.2 mol/L)was added thereto. The mixed solution was extracted with chloroformthree times. The organic phase was combined, and dried over anhydroussodium sulphate. The desiccant was removed by filtration. The filtratewas concentrated, and then subjected to column chromatography by usingtrichloromethane/methanol ( 1/20 in volume) as the eluent to give 549 mgof the compound having the structure of formula (X) with a yield of 95%.

The structure of the resultant compound having the structure of formula(X) was characterized by NMR, mass spectrometry and elemental analysis.The results were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.82-8.77 (m, 2H), 8.55 (d, J=8.0 Hz, 1H),8.50 (s, 1H), 8.22-8.16 (m, 5H), 8.13 (d, J=8.2 Hz, 1H), 8.01-7.97 (m,2H), 7.80 (s, 1H), 7.78 (t, J=7.8 Hz, 1H), 7.61 (d, J=8.28 Hz, 2H), 7.13(d, J=8.4 Hz, 2H), 5.09 (d, J=7.6 Hz, 2H), 4.01 (d, J=5.2 Hz, 2H),2.70-2.53 (m, 4H), 2.09-2.02 (m, 1H), 1.89 (br, 1H), 1.58-1.52 (m, 4H),1.46-1.29 (m, 32H), 1.16-1.12 (m, 18H), 1.04 (br, 14H), 0.93-0.89 (m,10H), 0.82-0.74 (m, 6H), 0.69 (t, J=6.1 Hz, 6H). ¹³C NMR (100 MHz,THF-d₈) δ: 167.75, 160.09, 156.17, 154.91, 153.62, 145.34, 142.30,142.23, 140.84, 138.67, 135.16, 134.47, 134.40, 132.27, 132.18, 131.97,131.33, 131.25, 131.07, 130.70, 129.84, 129.65, 129.25, 129.13, 126.12,125.80, 125.66, 125.58, 125.28, 124.82, 123.30, 122.51, 121.94, 121.49,119.15, 118.87, 116.14, 115.41, 71.64, 57.15, 54.18, 40.68, 40.47,39.33, 33.05, 32.90, 32.63, 31.24, 31.13, 30.90, 30.81, 30.61, 30.46,30.40, 28.02, 25.42, 23.77, 23.65, 23.55, 14.69, 14.64, 14.58, 14.51.

The results of high resolution mass spectrometry: 1377.86678.

The results of elemental analysis: C, 80.14; H, 8.69; N, 3.10.

The above experimental results indicated that the compound representedby formula (X) was prepared in the present invention.

EXAMPLE 2 Preparation of the Compound Having the Structure of Formula(XI)

Preparation of the compound having the structure of formula (XXIII-2):

In a dry Schlenk flask, of the compound having the structure of formula(XVI-2) (340 mg) was dissolved in 20 mL 1,2-dichloroethane. The reactionsystem was cooled to 0° C. with an ice bath. 0.15 mL of N, N-dimethylformamide and 0.046 mL phosphorus oxychloride were added to the reactionsystem. The mixture was stirred at 40° C. overnight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixture wasstirred for 2 hours, and then extracted with chloroform three times. Theorganic phase was combined, and dried over anhydrous sodium sulphate.The desiccant was removed by filtration. The filtrate was concentrated,and then subjected to column chromatography by using ethylacetate/petroleum ether ( 1/20 in volume) as the eluent to give 294 mgof the compound having the structure of formula (XXIII-2) with a yieldof 85%.

The structure of the compound having the structure of formula (XXIII-2)was characterized by NMR, mass spectrometry and elemental analysis. Theresults were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 9.97 (s, 1H), 8.81 (d, J=7.7 Hz, 1H), 8.79(d, J=7.6 Hz, 1H), 8.48 (d, J=8.1 Hz, 1H), 8.16 (d, J=8.2 Hz, 1H), 7.99(t, J=7.9 Hz, 1H), 7.05 (s, 1H), 7.91 (s, 1H), 7.79 (t, J=7.8 Hz, 1H),7.62 (d, J=8.4 Hz, 2H), 7.14 (d, J=8.4 Hz, 2H), 5.08 (d, J=7.7 Hz, 2H),3.99 (d, J=5.2 Hz, 2H), 2.60-2.59 (m, 3H), 1.87-1.86 (m, 1H), 1.57-1.55(m, 4H), 1.51-1.45 (m, 6H), 1.35-1.25 (m, 24H), 1.15-1.04 (m, 36H),0.92-0.86 (m, 10H), 0.82-0.75 (m, 12H). ¹³C NMR (100 MHz, THF-d₈) δ:182.59, 160.21, 155.22, 152.05, 146.34, 143.45, 139.68, 135.08, 134.92,132.70, 132.14, 131.72, 131.09, 129.91, 129.24, 126.72, 125.88, 125.79,125.60, 122.92, 122.37, 121.89, 120.19, 118.59, 116.18, 115.45, 71.67,56.96, 54.19, 40.67, 40.15, 39.32, 33.06, 33.04, 33.00, 32.92, 32.86,32.62, 31.22, 31.01, 30.89, 30.77, 30.55, 30.50, 30.35, 28.02, 27.94,23.77, 23.75, 23.62, 23.56, 14.68, 14.61, 14.54.

The results of mass spectrometry: 1152.85 ([M+H]⁺).

The results of elemental analysis: C, 83.35; H, 9.88; N, 1.21.

Synthesis of the compound having the structure of formula (XI):

In a dry two-necked round-bottom flask, the compound having thestructure of formula (XXIII-2) (250 mg) was dissolved in a mixed solventof acetonitrile and dichloromethane (½ in volume). Then cyanoacrylic (94mg) acid and ammonium acetate (55 mg) were added thereto. The reactionsystem was stirred at refluxor 48 hours.

After completion of the reaction, the temperature of the reaction systemwas cooled to the room temperature. After the addition of 30 mLdistilled water, the mixture was extracted with chloroform three times.The organic phases were combined, and dried over anhydrous sodiumsulphate. The desiccant was removed by filtration. The filtrate wasconcentrated, and then subjected to column chromatography by usingmethanol/chloroform ( 1/20 in volume) as the eluent to give the compoundhaving the structure of formula (XI). Thereafter, the compound havingthe structure of the structure s of formula (XI) was dissolved inchloroform. The mixture was washed with 0.2 mol/L of aqueous phosphoricacid solution and distilled water sequentially for several times. Theorganic phase was concentrated, and dried under reduced pressure to give251 mg of the compound having the structure of formula (XI) as a purplesolid with a yield of 98%.

The structure of the resultant compound having the structure of formula(XI) was characterized by NMR, mass spectrometry and elemental analysis.The results were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.87 (d, J=7.7 Hz, 1H), 8.83 (d, J=7.6 Hz,1H), 8.49-8.47 (m, 2H), 8.15 (d, J=8.2 Hz, 1H), 8.06 (t, J=7.8 Hz, 1H),7.98 (s, 1H), 7.89 (s, 1H), 7.81 (t, J=7.9 Hz, 1H), 7.61 (d, J=8.6 Hz,2H), 7.13 (d, 8.6 Hz, 2H), 5.06 (d, J=7.9 Hz, 2H), 4.01 (d, J=5.5 Hz,2H), 2.57-2.52 (m, 4H), 2.09-2.01 (m, 1H), 1.89-1.86 (m, 1H), 1.61-1.56(m, 4H), 1.45-1.29 (m, 32H), 1.14-1.04 (m, 32H), 0.92-0.85 (m, 10H),0.81-0.79 (m, 3H), 0.78-0.72 (m, 9H). ¹³C NMR (100 MHz, THF-d₈) δ:165.79, 160.23, 155.55, 152.84, 146.07, 143.33, 139.77, 139.49, 135.24,134.93, 133.04, 132.13, 131.77, 131.11, 130.70, 130.68, 130.36, 129.25,126.96, 125.91, 125.79, 125.59, 125.47, 123.12, 122.40, 122.04, 120.40,118.62, 118.37, 116.17, 115.45, 71.70, 56.91, 54.17, 46.11, 40.68,40.18, 39.33, 36.38, 33.07, 33.05, 32.97, 32.92, 32.87, 32.63, 31.23,31.02, 30.99, 30.89, 30.80, 30.71, 30.64, 30.55, 30.50, 30.42, 30.36,28.18, 28.03, 28.02, 27.92, 23.77, 23.75, 23.62, 23.57, 14.65, 14.63,14.59, 14.53.

The results of high resolution mass spectrometry: 1218.85502.

The results of elemental analysis: C, 81.72,; H, 9.42; N, 2.30.

The above experimental results indicated that the compound representedby formula (XI) was prepared in the present invention.

EXAMPLE 3

Synthesis of the compound having the structure of formula (XVI-3):

In a dry three-necked round-bottom flask, the compound having thestructure of formula (XIX-3) (1.43 g) was dissolved in 30 mL toluene.Then the solid acid catalyst Amberlyst 15 (600 mg) was added thereto.The mixture was stirred at reflux under the protection of argon gasovernight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with is chloroform three times. The organic phases werecombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using petroleum ether (boiling temperature:60-90° C.) as the eluent to give 421 mg of the compound having thestructure of formula (XVI-3) with a yield of 31%.

The structure of the resultant compound having the structure of formula(XVI-3) was characterized by NMR, mass spectrometry and elementalanalysis. The characterization data of NMR were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.71-8.67 (m, 1H), 8.63-8.60 (m, 11H), 8.08(d, J=8.2 Hz, 1H), 7.90 (s, 1H), 7.75-7.74 (m, 2H), 7.70-7.68 (m, 1H),7.60 (d, J=8.1 Hz, 2H), 7.34-7.33 (m, 1H), 7.19-7.17 (m, 1H), 7.09 (d,J=6.6 Hz, 2H), 4.62-4.58 (m, 2H), 3.96 (br, 2H), 2.36 (br, 1H),2.36-2.05 (m, 4H), 1.84 (br, 1H), 1.56 (br, 2H), 1.44 (br, 12H),1.35-1.28 (m, 20H), 1.22-1.13 (m, 18H), 1.05-0.99 (m, 14H), 0.93-0.89(m, 8H), 0.85-0.75 (m, 16H). ¹³C NMR (100 MHz, THF-d₈) δ: 159.95,144.35, 141.17, 139.28, 138.02, 135.40, 133.61, 132.16, 131.82, 129.39,128.96, 127.75, 126.22, 126.00, 125.41, 125.03, 124.75, 123.80, 123.34,122.31, 121.18, 118.27, 118.12, 115.33, 115.03, 106.23, 71.66, 50.50,49.37, 48.25, 40.91, 39.34, 33.06, 33.00, 32.96, 32.88, 32.73, 32.63,31.24, 31.11, 30.90, 30.78, 30.71, 30.51, 30.42, 30.33, 28.03, 27.51,27.44, 25.97, 23.77, 23.69, 23.58, 14.69, 14.60.

The results of mass spectrometry: 1124.85 ([M+H]⁺).

The results of elemental analysis: C, 84.34; H, 10.13; N, 1.24.

Synthesis of the compound having the structure of formula (XXIII-3):

In a three-necked round-bottom flask dried by flame, the compound havingthe structure of formula (XVI-3) (400 mg) was dissolved in 15 mLanhydrous tetrahydrofuran. The mixture was cooled to −78 ° C., and then0.33 mL t-butyl lithium (1.3 mol/L in n-hexane) was added thereto underthe protection of argon gas. The reaction was stirred at −78 ° C. for 1h, and then trimethyl tin chloride (85 mg) was added thereto. Themixture was stirred at room temperature overnight.

After completion of the reaction, 20mL water was added to the reactionsystem. The mixed solution was extracted with chloroform three times.The organic phase was combined, and dried over anhydrous sodiumsulphate. The desiccant was removed by filtration. The filtrate wasconcentrated to give a viscous liquid, which was directly used for thenext reaction.

Synthesis of the compound having the structure of formula (XII-3):

The compound having the structure of formula (XXIII-3) was dissolved in20 mL 1,4-dioxane after sufficiently drying. Then the compound havingthe structure of formula (XVIII-3) (250 mg) and catalyst Pd₂(PPh)₂Cl₂(30 mg) were added thereto under the protection of argon gas. Thereaction system was stirred at reflux overnight.

After completion of the reaction, the reaction system was cooled to theroom temperature, and 20 mL water was added thereto. The mixed solutionwas extracted with chloroform three times. The organic phase wascombined, and dried over anhydrous sodium sulphate. The desiccant wasremoved by filtration. The filtrate was concentrated, and then subjectedto column chromatography by using ethyl acetate/petroleum ether ( 1/20in volume) as the eluent to give 412 mg of the compound having thestructure of is formula (XII-3) with a yield of 81%.

The structure of the resultant compound having the structure of formula(XII-3) was characterized by NMR, mass spectrometry and elementalanalysis. The characterization data of NMR were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.79 (d, J=8.1 Hz, 1H), 8.68 (d, J=7.4 Hz,1H), 8.54 (m, 1H), 8.16-8.08 (m, 5H), 8.01 (d, J=6.4 Hz, 1H), 7.95 (s,1H), 7.90 (d, J=8.1 Hz, 1H), 7.80 (d, J=6.2 Hz, 1H), 7.74 (m, 1H), 7.62(s, 1H), 7.55 (d, J=8,4 Hz, 2H), 7.08 (d, J=8.6 Hz, 2H), 4.44 (m, 2H),4.36 (t, J=6.4 Hz, 2H), 3.98 (d, J=5.3 Hz, 2H), 2.50-2.40 (m, 2H), 2.31(m, 3H), 1.87 (m, 1H), 1.78 (m, 2H), 1.57-1.28 (m, 37H), 1.22 (m, 20H),1.06 (m, 18H), 0.92 (m, 8H), 0.79 (t, J=6.3 Hz, 6H), 0.70 (t, J=4.8 Hz,6H). ¹³C NMR (100 MHz, CDCl₃) δ: 166.51, 159.99, 154.84, 153.75, 145.60,142.47, 141.82, 140.91, 138.44, 137,53, 135.26, 133.83, 133.68, 132.17,131.72, 131.62, 131.12, 130.68, 130.42, 130.04, 129.71, 129.57, 129.40,129.22, 129.08, 128.25, 127.11, 126.30, 125.94, 125.63, 125.49, 124.98,124.93, 123.41, 122.58, 121.36, 118.59, 118.15, 115.31, 114.97, 106.95,71.69, 65.43, 50.59, 49.35, 48.42, 40.74, 39.36, 33.08, 33.06, 33.01,32.96, 32.89, 32.69, 32.63, 32.03, 31.24, 31.13, 30.91, 30.79, 30.70,30.51, 30.45, 30.38, 30.36, 28.05, 28.03, 27.43, 27.39, 26.17, 23.78,23.76, 23.70, 23.66, 23.55, 20.37, 14.47, 14.66, 14.62, 14.50, 14.35.

The results of mass spectrometry: 1435.95 ([M+H]⁺).

The results of elemental analysis: C, 80.34; H, 8.91; N, 2.91.

Synthesis of the compound having the structure of the structure offormula (XII):

In a three-necked round-bottom flask, the compound having the structureof formula (XII-3) (300 mg) was dissolved in 15 mL tetrahydrofuran and 5mL water. Then the potassium hydroxide (117 mg) was added to thereaction system. The mixture was stirred at 80° C. for 5 hours.

After completion of the reaction, the reaction system was cooled to theroom is temperature, and 20 mL of aqueous phosphoric acid solution (0.2mol/L) was added thereto. The mixed solution was extracted withchloroform three times. The organic phase was combined, and dried overanhydrous sodium sulphate. The desiccant was removed by filtration. Thefiltrate was concentrated, and then subjected to column chromatographyby using trichloromethane/methanol ( 1/20 in volume) as the eluent togive 274 mg of the compound having the structure of formula (XII) with ayield of 95%.

The structure of the compound having the structure of formula (XII) wascharacterized by NMR, mass spectrometry and elemental analysis. Theresults were as follows:

¹H NMR (400 MHz, THF-d₈) δ: 8.80 (d, J=8.0 Hz, 1H), 8.69 (d, J=7.5 Hz,1H), 8.53 (s, 1H), 8.21-8.16 (m, 5H), 8.09 (d, J=8.2 Hz, 1H), 8.06 (s,1H), 7.97 (d, J=7.5 Hz, 1H), 7.90 (d, J=8.0 Hz, 1H), 7.77-7.72 (m, 2H),7.60 (d, J=8.3 Hz, 2H), 7.10 (d, J=8.4 Hz, 2H), 4.69 (d, J=6.7 Hz, 2H),4.00 (d, J=5.3 Hz, 2H), 2.43-2.29 (m, 6H), 2.08-2.02 (m, 1H), 1.88-1.84(m, 1H), 1.57-1.46 (m, 14H), 1.36-1.26 (m, 30H), 1.19-1.14 (m, 8H), 1.05(br, 18H), 0.93-0.89 (m, 6H), 0.80-0.77 (m, 6H), 0.70 (t, J=6.5 Hz, 6H).¹³C NMR (100 MHz, THF-d₈) δ: 167.73, 159.96, 154.82, 153.73, 145.59,142.19, 141.74, 140.93, 138.39, 137.59, 135.24, 133.78, 133.67, 132.16,131.72, 131.57, 130.73, 129.96, 129.49, 129.38, 129.16, 129.06, 128.11,127.13, 126.29, 125.92, 125.63, 125.49, 124.92, 123.41, 122.57, 121.36,118.55, 118.13, 115.31, 114.94, 106.93, 71.67, 50.56, 49.34, 48.42,40.70, 39.34, 33.05, 32.99, 32.94, 32.88, 32.62, 31.23, 32.12, 30.90,30.77, 30.69, 30.50, 30.40, 30.36, 28.03, 27.40, 26.19, 23.76, 23.69,23.54, 14.67, 14.51.

The results of high resolution mass spectrometry: 1377.86678.

The results of elemental analysis: C, 80.14; H, 8.69; N, 3.10.

The above experimental results indicated that the compound representedby formula (XII) was prepared in the present invention.

EXAMPLE 4

An organic dye-sensitized solar cell was assembled in accordance withthe document (Energy Environ. Sci., 2010,3, 1924), specifically asfollows.

The organic dyes produced in Examples 1 to 3 (i.e. the compound havingthe structure of formula (X), the compound having the structure offormula (XI) and the compound having the structure of formula (XII))were prepared into a 150 μmol/L ethanol/toluene (9/1 in volume)solution, respectively.

A bilayer membrane electrode with a TiO₂ structure was immersed in thesolution for 12 hours. Then, the electrode was taken out. A glasselectrode coated with nanoplatinium was sealed annularly by a hot meltmethod. At last, an electrolyte was filled into the gap between the twoelectrodes, thereby dye-sensitized solar cells were constructed.

Under the simulated AM1.5G sunlight at 100 mW cm⁻², the produceddye-sensitized solar cells were detected for the performance. The testresults are in Table 1. Table 1 shows the results of the performancetests of the dye-sensitized solar cells made from the organic dyesaccording to the Examples of the invention.

TABLE 1 the results of the performance tests of the dye-sensitized solarcells made from the organic dyes according to the examples of theinvention Organic Short circuit Open circuit Filling Cell Efficiencydyes current [mA cm⁻²] voltage [mV] factor [%] X 17.95 850 0.740 11.5 XI13.69 832 0.758 8.63 XII 17.64 823 0.724 10.5

The description of the above Examples is only for the purpose of helpingthe reader to understand the process of the present invention and thekey idea thereof. It should be understood that many changes andmodifications may be made by those skilled in the art without deviatingfrom the principle of the present invention. Those changes andmodifications also fall into the protection scope of the claims of thepresent invention.

1. An organic dye having the structure of formula (I) or formula (II):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl; R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula (IV), formula (V) or formula (VI):

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; x is 0 or 1; R₁₋₅, and R₂₋₅ are independently selected from H, aryl or C₁-C₃₆ alkyl.
 2. The organic dye according to claim 1, wherein the aryl is aryl substituted with C₁-C36 alkyl or aryl substituted with C₁-C₃₆ alkoxy.
 3. The organic dye according to claim 1, wherein the aryl is selected from formula (VII), formula (VIII) or formula (IX):

wherein R₈ is H, C₁-C₃₆ alkyl or C₁-C₃₆ alkoxy; R₉, R₁₀, and R₁₁ are independently selected from H or C₁-C₃₆ alkyl; y is 0 or
 1. 4. The organic dye according to claim 1, wherein said R₁₋₁, and R₂₋₁ are independently selected from C₃-C₃₀ alkyl.
 5. The organic dye according to claim 1, wherein said R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₃-C₃₀ alkyl, phenyl substituted with C₃-C₃₀ alkyl or phenyl substituted with C₃-C₃₀ alkoxy.
 6. The organic dye according to claim 1, wherein said organic dye has the structure of formula (X), formula (XI) or formula (XII):


7. A process for producing an organic dye comprising: 1) reacting a compound having the structure of formula (XIII) with a compound having the structure of formula (XIV) to give a compound having the structure of formula (XV),

wherein R₁ is C₁-C₃₆ alkyl; R₅ is H, aryl or C₁-C₃₆ alkyl; R₁₂ is C₁-C₈ alkyl; 2) converting the compound having the structure of formula (XV) into a to compound having the structure of formula (I) or formula (II):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl; R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; R₁₋₄, and R₂₋₄ are independently selected from formula (III), formula (IV), formula (V) or formula (VI):

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; x is 0 or 1; R₁₋₅, and R₂₋₅ are selected from hydrogen, aryl or C₁-C₃₆ alkyl.
 8. The process according to claim 7, wherein said step 2) specifically is as follows: 2-1) converting the compound having the structure of formula (XV) into a compound having the structure of formula (XVI) or formula (XVII):

wherein R₁₋₁, and R₂₋₁ are independently selected from C₁-C₃₆ alkyl; R₁₋₂, R₁₋₃, R₂₋₂, and R₂₋₃ are independently selected from H, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; R₁₋₅, and R₂₋₅ are selected from H, aryl or C₁-C₃₆ alkyl; 2-2) reacting the compound having the structure of formula (XVI) or formula (XVII) with a compound having the structure of formula (XVIII) to give the compound having the structure of formula (I) or formula (II); R₄-X (XVIII), wherein R₄ is the formula (III), formula (IV), formula (V) or formula (VI),

wherein R₆, and R₇ are independently selected from H, F, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; x is 0 or 1; X is H, Br or I.
 9. The process according to claim 8, wherein said step 2-1) specifically is as follows: 2-1-1) converting the compound having the structure of formula (XV) into a compound having the structure of formula (XIX):

wherein R₁ is C₁-C₃₆ alkyl; R₂, and R₃ are independently selected from H, C₁-C₃₆ alkyl, phenyl substituted with C₁-C₃₆ alkyl or phenyl substituted with C₁-C₃₆ alkoxy; R₅ is H, aryl or C₁-C₃₆ alkyl; 2-1-2) converting the compound having the structure of formula (XIX) into the compound having the structure of formula (XVI) or formula (XVII).
 10. A dye-sensitized solar cell comprising an organic dye layer, wherein the organic dye layer comprises the organic dye according to claim
 1. 